PDSS2 Gene Coenzyme Q10 Deficiency Type 3 NGS Genetic DNA Test
Introduction
The PDSS2 Gene Coenzyme Q10 Deficiency Type 3 NGS Genetic DNA Test is a cutting-edge diagnostic tool that plays a vital role in identifying genetic mutations associated with Coenzyme Q10 deficiency, a condition linked to various neurological disorders. This test employs Next-Generation Sequencing (NGS) technology to provide precise insights into the genetic factors that may contribute to your health issues.
What the Test Measures
This test specifically measures mutations in the PDSS2 gene, which are critical for the synthesis of Coenzyme Q10, a vital component for cellular energy production. By identifying these mutations, healthcare providers can better understand the underlying causes of neurological symptoms.
Who Should Consider This Test?
- Individuals with a family history of neurological disorders.
- Patients experiencing symptoms such as muscle weakness, seizures, or developmental delays.
- Those with unexplained neurological issues that may be linked to genetic factors.
Benefits of Taking the Test
- Accurate identification of genetic mutations that may lead to Coenzyme Q10 deficiency.
- Informed decision-making regarding treatment options and management strategies.
- Enhanced understanding of familial risks and implications for family members.
Understanding Your Results
Results from the PDSS2 Gene Coenzyme Q10 Deficiency Type 3 NGS Genetic DNA Test will provide insights into the presence of specific genetic mutations. A genetic counselor will assist you in interpreting these results, discussing their implications for your health and your family’s health.
Test Pricing
| Price Type | Amount (NGN) |
|---|---|
| Discount Price | 400,000 NGN |
| Regular Price | 560,000 NGN |
Booking Information
To book the PDSS2 Gene Coenzyme Q10 Deficiency Type 3 NGS Genetic DNA Test, please contact us at +2348077798758 or visit our website. Ensure you have a clinical history prepared and consider a genetic counseling session to draw a pedigree chart of affected family members prior to testing.
Turnaround Time: 3 to 4 Weeks
Sample Type: Blood or Extracted DNA or One drop Blood on FTA Card
Specialty: Neurology
Department: Genetics
Method: NGS Technology
Disease Type: Neurological Disorders
